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Treatment-free survival outcomes from the phase II study of nivolumab and salvage nivolumab/ipilimumab in advanced clear cell renal cell carcinoma (HCRN GU16-260-Cohort A).
Atkins, Michael B; Jegede, Opeyemi A; Haas, Naomi B; Mcdermott, David F; Bilen, Mehmet A; Stein, Mark; Sosman, Jeffrey; Alter, Robert; Plimack, Elizabeth R; Ornstein, Moshe C; Hurwitz, Michael; Peace, David J; Einstein, David; Catalano, Paul J; Hammers, Hans; Regan, Meredith M.
Afiliación
  • Atkins MB; Oncology, Georgetown University Medical Center, Washington, District of Columbia, USA mba41@Georgetown.edu.
  • Jegede OA; Biostatistics, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • Haas NB; Medicine, University of Pennsylvania Health System, Philadelphia, Pennsylvania, USA.
  • Mcdermott DF; Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
  • Bilen MA; Department of Hematology and Medical Oncology, Emory University Winship Cancer Institute, Atlanta, Georgia, USA.
  • Stein M; Columbia University, New York, New York, USA.
  • Sosman J; Columbia University/Herbert Irving Cancer Center, New York, New York, USA.
  • Alter R; Northwestern University Department of Medicine, Chicago, Illinois, USA.
  • Plimack ER; John Theurer Cancer Center, Hackensack, New Jersey, USA.
  • Ornstein MC; Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA.
  • Hurwitz M; Taussig Cancer Institute, Cleveland, Ohio, USA.
  • Peace DJ; Medical Oncology, Yale School of Medicine, New Haven, Connecticut, USA.
  • Einstein D; Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
  • Catalano PJ; Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
  • Hammers H; Biostatistics, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • Regan MM; The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
J Immunother Cancer ; 12(4)2024 Apr 11.
Article en En | MEDLINE | ID: mdl-38604810
ABSTRACT

BACKGROUND:

As part of a partitioned survival analysis, treatment-free survival (TFS) can characterize the overall survival time patients spend between the cessation of immunotherapy and the start of subsequent therapy; both with and without toxicity. Significant TFS was reported for the nivolumab/ipilimumab arms of the CheckMate 067 and 214 trials for patients with advanced melanoma or renal cell carcinoma (aRCC), respectively, where immunotherapy was often halted for toxicity rather than a predefined treatment endpoint. We therefore sought to assess TFS in the HCRN GU16-260 trial, which was designed to reduce toxicity and cap immunotherapy duration.

METHODS:

Data were analyzed from 128 patients with clear-cell aRCC treated with first-line nivolumab monotherapy for up to 2 years. Salvage nivolumab/ipilimumab for up to 1 year was provided to eligible patients with disease progression at any point or stable disease at 48 weeks (29% of patients). TFS was defined as the area between Kaplan-Meier curves for a time from registration to protocol therapy cessation and for a time from registration to subsequent systemic therapy initiation or death, estimated from 36-month mean times. The time on or off protocol treatment with grade 3+treatment-related adverse events (TRAEs) was also captured.

RESULTS:

At 36 months from enrollment, 68.3% of patients were alive 96.8% of International Metastatic RCC Database Consortium (IMDC) favorable-risk patients and 56.6% of those with intermediate/poor-risk, respectively. The 36-month mean time on protocol therapy was 11.5 months including 0.6 months with grade 3+TRAEs (16.0 months for favorable-risk patients and 9.6 months for intermediated/poor-risk patients). The 36-month mean TFS for the whole population was 9.4 months (12.9 months including 1.5 months with grade 3+TRAEs for favorable-risk and 8.0 months including 1.0 months with grade 3+TRAEs for intermediate/poor-risk). At 36 months, 65.6% of favorable-risk patients and 27.1% of intermediate/poor-risk patients were alive and subsequent systemic treatment-free.

CONCLUSIONS:

Nivolumab monotherapy with salvage nivolumab/ipilimumab in non-responders is an active treatment approach in treatment-naïve patients with aRCC and, similar to nivolumab/ipilimumab in CheckMate 214, results in substantial TFS and toxicity-free TFS. TFS was greatest in patients with favorable-risk disease, supporting the use of an immunotherapy-only regimen in this population.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Neoplasias Renales / Melanoma Límite: Humans Idioma: En Revista: J Immunother Cancer Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Neoplasias Renales / Melanoma Límite: Humans Idioma: En Revista: J Immunother Cancer Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido